{
  "id": 13365,
  "label": "parietal foramina 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012309",
  "properties": {
    "xrefs": [
      "GARD:0018053",
      "MEDGEN:355358",
      "MESH:C566510",
      "OMIM:609597",
      "UMLS:C1865044"
    ],
    "synonyms": [
      "ALX4 parietal foramina",
      "parietal foramina 2",
      "parietal foramina caused by mutation in ALX4",
      "parietal foramina type 2",
      "PFM2"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any parietal foramina in which the cause of the disease is a mutation in the ALX4 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18875,
      "label": "parietal foramina",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18236,
        18360,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060285",
          "GARD:0016662",
          "HP:0002697",
          "MESH:C566826",
          "OMIMPS:168500",
          "Orphanet:60015",
          "SCTID:718099006",
          "icd11.foundation:905361904"
        ],
        "synonyms": [
          "catlin marks",
          "enlarged parietal foramina",
          "fenestrae parietales symmetricae",
          "foramina parietalia permagna",
          "hereditary cranium bifidum",
          "parietal foramina",
          "symmetric parietal foramina"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Enlarged parietal foramina (EPF) is a developmental defect, characterized by variable intramembranous ossification defects of the parietal bones, which is either asymptomatic, symptomatic (headaches, nausea, vomiting, intellectual disability) or associated with other pathologies."
      },
      "child_count": 9,
      "reference_id": "MONDO:0018953"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18875,
      "label": "parietal foramina"
    }
  ]
}